A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048094



Internal ID19137313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4486982..4528582hg38UCSC Ensembl
Innerchr11:4508212..4549812hg19UCSC Ensembl
Innerchr11:4464788..4506388hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3841601
hg1941601
hg1841601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510557
Samples
Known GenesOR52K1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048094
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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